Control of reproductive cycle with 6-chloro - 17 alpha-hydroxy-4,6-pregnadiene-3,20-dione-17-acetate



United States Patent CONTROL OF REPRODUCTIVE CYCLE WITH 6- CHLORO 17 ALPHA-HYDROXY-t,G-PREGNADI- ENE-3,20-DIONE-17-ACETATE John C. Babcock and J Allan Campbell, Kalamazoo, Mich., assignors to The Upjohn Company, Kalamazoo, Mich., a corporation of Delaware No Drawing. Continuation-impart of application Ser. No. 814,153, May 19, 1959. This application Mar; 25, 1963, Ser. No. 267,774

Int. Cl. A61r 17/06 US. Cl. 424243 Claims ABSTRACT OF THE DISCLOSURE Compositions and methods of use thereof embody 6u-chloro-l7a-hydroxy-4-pregnene-3,ZO-dione l7-acetate or 6-chloro-17a-hydroxy-4,6-pregnadiene-3,20-dione 17- acetate. Oral and parenteral compositions are provided. Methods of oral and parenteral administration are beneficial in mammals, e.g., humans and animals, and in birds to inhibit ovulation, to forestall abortion, to control estrual and anestrual periods, and to control moulting and egg laying.

This invention relates to pharmaceutical compositions and uses thereof and more particularly to steroid pharmaceutical compositions and to the use thereof in the treatment of mammals and birds.

The invention provides novel compositions comprising pharmaceutically acceptable carriers and as the essential active ingredient a member selected from the group consisting of 6ot-chloro-17ot-hydroxy-4-pregnene-3,ZO-dione 17-acetate and 6-chloro-17a-hydroxy-4,6-pregnadiene-3, 20-dione 17-acetate and methods of treatment therewith. The said essential active ingredients can be prepared according to the processes disclosed in copending U.S. patent application Ser. No. 814,153, filed May 19, 1959, now abandoned of which this application is a continuation in part.

The modes contemplated by the inventors of carrying out the invention includes pharmaceutical compositions suited for oral administration, pharmaceutical compositions suited for injection, implantable pellets, and methods of systemic administration thereof.

The compositions suited for oral administration include solid and liquid compositions. The solid oral compositions can be in the form of tablets, scored and unscored, coated and uncoated; capsules, hard and soft; powders; granules; pills; and the like. Solid diluents and carriers suited for such compositions are selected from the group consisting of lipids, carbohydrates, proteins and mineral solids. The liquid oral compositions can be in the form of dispersions, suspensions, and syrups.

Tablets contain the essential active ingredient in the required amount with pharmaceutically acceptable diluents, excipients, binders, disintegrators and lubricants. The essential active ingredient is preferably mixed with a carbohydrate diluent, for example, starch and sucrose; a mineral solid, for example, terra alba (calcium sulfate) and dicalcium phosphate; or the like, to form a basic powder mixture. The said mixture can be granulated by wetting with a protein binder such as gelatin solution, a carbohydrate such as starch paste, syrup, and acacia mucilage; and screened. As an alternative to granulating, the mixture can be slugged and the slugs broken down into granules prior to formation of the tablets. A carbohydrate disintegrator, for example, corn starch is ad- 3,511,913 Patented May 12, 1970 vantageously added at the time of forming the basic mixture. The lubricant, for example, a lipid such as stearic acid, a stearate salt and mineral oil; a mineral solid such as talc; and the like, is used to prevent sticking of the mixture to the tablet forming dies. The said tablets can be coated or uncoated. Suitable coatings include a sealing coat of shellac, a taste-disguising carbohydrate coating such as sugar and methyl cellulose, and a lipid polish coating of, for example, carnauba wax. The coating can comprise (a) lipid type coatings of a semipermeable nature for delaying absorption of the essential active ingredient to provide sustained action, or (b) enteric substances such as styrene maleic acid copolymer and cellulose acetate phthalate to resist released of the essential active ingredient in the stomach and permit release in the upper intestine.

The capsules for oral use comprise the essential active ingredients in combination with a pharmaceutically acceptable diluent or excipient and a formed gelatin enclosure for the composition. The capsules can be in the form of soft capsules enclosing the active ingredient in the required amount with suitable diluents, for example, edible oils. The diluents for hard capsules comprise mineral solids, for example, talc, dicalcium phosphate, and the like; carbohydrates, for example, starch, sucrose and lactose; and as required, lubricants, for example, stearate salts.

The powders can be advantageously and conveniently prepared by comminuting the essential active ingredient in the required amount and mixing with a pharmaceutically acceptable diluent; for example, an edible carbohydrate such as starch, advantageously including sweetening and flavoring agents, for example, sugar, saccharin, cyclamate or its salts; and flavoring oils.

For the treatment of domestic birds and animals and laboratory animals by oral administration the essential active ingredient is conveniently incorporated into animal and bird feed carriers to compound pre-mix and ready-mix type products. The feed carriers comprise in balanced amounts the essential dietary constituents, protein, fat, carbohydrate, minerals, and the like. Premixes, for extemporaneous addition to animal and bird rations, contain ingesti'ble bulking agents and diluents which can be dietary constituents, and the essential active ingredient in a concentration suited for the addition of the said ingredients in amounts calculated on the weight of the animal or bird under treatment. The ready-mixed type is prepared by incorporating the essential active ingredient directly into the bulk ration.

As set forth above, the liquid oral compositions can be in the form of dispersions, suspensions, and syrups.

Dispersions can be prepared in glycerol, propylene glycol, liquid polyethylene glycols, and mixtures thereof, and in edible oils. Under ordinary conditions of storage and use, such preparations contain a preservative to prevent the growth of microorganisms. Likewise, sweetening, coloring, and flavoring agents can be added.

Suspensions are prepared in an aqueous vehicle containing diluents, flavors, and preservatives as requiredv The syrups contain the essential active ingredient in the required amount in an aqueous medium containing a sweetening agent, for example, sugar, saccharin, or cyclamate salts. Colors, flavors and preservatives are added for convenient storage and use.

As stated above, the pharmaceutical compositions can be in forms suited for injection use, which forms include sterile aqueous suspensions and sterile powders for the extemporaneous preparation of sterile injectable suspensions. In all cases the form must be sterile and must be fluid to the extent that easy syringeability exits. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi. The basic dispersion medium can contain water, ethanol, polyols (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof and vegetable oils. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size for suspensions and by the use of surfactants (for example, a condensation product of ethylene oxide with fatty acids or fatty alcohols, partial esters of fatty acids and a hexitol anhydride, and polyoxyethylene condensation products of the esters). The deleterious action of microorganisms can be prevented by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, benzyl alcohol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monosterate and gelatin.

Generally, suspensions are prepared by incorporating the previously sterilized essential active ingredient into a sterile vehicle which contains the basis dispersion medium and the required other ingredients from those enumerated above.

The essential active ingredient can be sterilized by the use of a gas, for example, ethylene oxide. With the required additional ingredients and in the proper particle size, the sterilized ingredient can be compounded into a sterile powder for later extemporaneous reconstitution with a desired suspending liquid, which, of course, itself must be sterile.

It is especially advantageous to compound the inventive compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used in the specification and claims herein refers to physically discrete units suited as unitary dosages for animal, bird, and human subjects, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect in association with a suitable pharmaceutical carrier. The specifications for the novel dosage unit forms of this invention are dictated by and directly dependent on (a) the unique characteristics of the active material and the particular therapeutic effect to be achieved and (b) the limitations inherent in the art of compounding such an active material for therapeutic use in animal, bird, and human subjects as disclosed in detail in this specification, these being features of the present invention. Examples of the dosage unit forms heretofore described are premixes, boluses, tablets, capsules, pills, powder packets, wafers, cachets, teaspoonfuls, dropperfuls and tablespoonfuls, implantable pellets, vials, ampuls, and segregated multiples thereof, and other forms alluded to herein. Drop dosage forms are well suited for use in birds and poultry.

The inventive compositions are administered in varying dosages depending on the weight and condition of the mammals and birds under treatment, the route of administration, i.e., oral administration or parenteral injection, the particular condition to be treated and the nature of the desired results.

The total daily dosage of active ingredient per pound of the treated subject varies from about 0.2 milligram to about 2 milligrams. Thus, over the weight range of about 5 pounds for a small dog to about 1000 pounds for a mare, the daily dosage ranges from about 1 milligram to about 2000 milligrams of the active ingredient.

The said dosages can be administered, for example, in the form of an ingestible pre-mix containing by weight from about 0.00004% to about 1% of the essential active ingredient; in the form of a sterile injectable suspension containing by weight/ volume from about 0.5% to about 25%; in the form of an implantable pellet containing from about 1 mg. to about 250 milligrams; in the form of an ingestible bolus containing from about 50 mgs. to about 1000 milligrams; in the form of an aqueous oral suspension containing by weight/volume from about 0.005% to about 5%; in the form of an ingestible readymix feed composition containing by weight from about 0.000002% to about 0.008%; and in the form of an oral tablet or capsule containing from about 1 mg. to about 500 milligrams.

The compositions of the present invention are novel and useful pharmaceutical preparations demonstrating unexpected, advantageous and beneficial results in the treatment of ovulating mammals and birds, for example, by re establishing normal endometrium-ovary-anterior pituitary relationships, by forestalling habitual and threatened abortion, by easing pre-menstrual tension, by preventing ovulation, in treating endometriosis and dysmenorrhea, and in delaying menstruation. In the practice of veterinary medicine, the compositions provide beneficial and advantageous results in the hormonal control of the reproductive cycle in animals, for example, by reducing the postpartum anestrual period in cattle; by increasing in animals the number of implanted fertilized ova, of live births and the viability thereof; by synchronization of the estrual period in a group of swine, cattle, horses, sheep, dogs or cats; by preventing estrual activity in fattening meat animals; by initiating cyclic activity in normal but noncycling animals; by controlling the estrual period in individual animals; by shortening pseudopregnancy in dogs; and by providing compositions and methods to further weight gain with lessened side effects in beef cattle. In birds, there are provided compositions and methods to interrupt broodiness in laying hens, to control the moulting period and the egg laying period of a flock, and to increase the number of eggs. The species variations in the estrual periods of the mammals must be taken into account in the several uses of the inventive compositions. When cycling, cows, horses, sheep, swine, and cats have normal estrual periods from about 15 to about 23 days apart; dogs about 6 months apart. Thus, the treatment to synchronize the estrual period, whether oral or injectable, is continued for a maximum number of days ascertainable by reference to the normal length of the estrual period of the particular species. Prolonged prevention of the estrual periods is brought about by continued oral treatment or spaced administration of injectable suspensions with a prolonged etfect.

The following examples include the best mode contemplated by the inventor of carrying out the invention and are not to be construed as limiting.

EXAMPLE 1 Injectable suspension 10,000 mls. of a sterile aqueous suspension are pre pared from the following types and amounts of ingredients:

Each ml.: Total, gms. 6 chloro-17a-hydroxy-4,6-pregnadiene-3,20-dione 17-acetate (25 mgs.) 250 Sodium chloride (9 mgs.)

Water for injection U.S.P. (q.s.) ad. 10,000 mls.

The sodium chloride and a preservative are dissolved in the Water and the whole is sterilized by passage through a sterilizing filter. The active ingredient is micronized, sterilized by exposure to sterilizing vapor and added aseptically to the sterile aqueous solution. Dispersion is accomplished by passing through'a sterile homogenizer. The final suspension is filled aseptically into sterile vials.

The duration of action of the injected suspension is prolonged. The single injection of 4 mls. per animal in a group of beef cattle is effective in preventing estrus for from about 50 to about days.

5 EXAMPLE 2 Oral suspension 4000 mls. of a fluid drop preparation suitable for the addition of measured amounts to animal feed is prepared from the following types and amounts of ingredients:

Preservativel4 gms.

Surfactant-3.6 gms.

6 chloro-l7a-hydroxy-4,6-pregnadiene-3,20-dione 17-acetate--l gms.

Purified water U.S.P., q.s. ad.4000 mls.

The preservative is added to 500 mls. of the water at about 55 C. The surfactant is added followed by the micronized active ingredient. The whole is made up to volume with the balance of the water and passed through an homogenizer.

For control of the estrual period of a 10 kilo bitch, 2 ml. is added daily to the animal ration, providing a daily dosage of mgs. of the steroid acetate equivalent to 0.5 mg. per kilo of dog weight per day. After cessation of treatment the animal comes into heat and can be bred successfully.

For synchronization of the moulting period in poultry, 400 mls. is mixed daily into 50 lbs. of feed mash for a flock of 100 heavy breed (5.5 lbs.) hen chickens, providing a daily dosage in one-half pound of the mash of mgs. of the steroid acetate equivalent to about 4 mgs. per kilo of hen weight per day. After cessation of treatment the chickens begin to lay concurrently.

EXAMPLE 3 Ready-mix feed composition A mash feed mix for hen chickens is prepared from the following types and amounts of materials:

Laying mashl00 lbs. 6-chloro-17a-hydroxy-4,6-pregnadiene-3,20-dione 17-acetate (micronized)2 gms.

The active ingredient is micronized and worked into a portion of the mash by careful mixing, and the mix is incorporated uniformly into the remaining mash. Each pound of the finished preparation contains 20 mgs. of the steroid acetate, providing a daily dose of 10 mgs. for a heavy breed hen eating one-half pound of the mash per day. This daily dose is effective in controlling the moulting period.

EXAMPLE 4 Implantable composition 10,000 pellets for implantation in beef cattle are prepared from the following types and amounts of materials:

6 chloro-l7u-hydroxy-4,6-pregnadiene-3,20-dione 17-acetate--1000 gms.

The active ingredient is blended with an inert diluent into a uniform mixture. The mixture is slugged and screened to a granular consistency. A lubricant is added and the granules are compressed into pellets, each containing 100 mgs. of the progestational compound.

Good results in the weight increase of growing beef cattle are obtained by implantation of one pellet at the time the cattle go on full feed for fattening.

EXAMPLE 5 Ingestible pre-mix 10,000 gms. of a pre-mix is prepared from the following types and amounts of ingredients:

6-chloro-17a-hydroxy-4,6-pregnadiene 3,20 dione 17- acetate-20 gms.

Soybean meal9980 gms.

Chloroform, U.S.P.-1500 mls.

A chloroform solution of the active ingredient is prepared and incorporated gradually and uniformly into the soybean meal. After adequate mixing the whole is dried to remove any trace of chloroform.

Each gram of the pre-mix contains 2 mgs. of the steroid acetate. Two kilograms of the pre-mix is added to 1 ton of the standard ratio of a group of gilts to provide 2 mgs. per pound of feed which furnishes a daily dose to each gilt of 10 mgs. of the steroid acetate when the animal is fed at the rate of 5 lbs. finished feed per day. Treatment throughout gestation results in an increased number of pigs at farrowing.

An equally satisfactory pre-mix is prepared by omitting the chloroform, grinding the active ingredient into a fine powder, which is added to the soybean meal with mixing, and using mineral oil as an antidust. This gives a uniform pre-mix which is well suited for later incorporation into the animal ration.

EXAMPLE 6 Bolus 9000 boluses, each containing 75 mgs. of the steroid acetate, are prepared from the following types and amounts of ingredients:

6-chloro-17a-hydroxy-4,6-pregnadiene 3,20 dione 17- acetate-675 gms. Lactose-69,265 gms.

The above ingredients are blended and granulated with syrup-starch paste. The granulation is then dried, lubricated with starch, talc and calcium stearate powders, and compressed.

The oral administration to a cycling mare of four boluses per day is effective in the control of estrus. The treatment is especially advantageous in racing mares.

EXAMPLE 7 Tablet 10,000 compressed tablets are prepared from the following types and amounts of ingredients:

Each tablet:

6-ch1oro-l7a-hydroxy-4,G-pregnadiene 3,20 dione 17-acetate (1 mg.)-10 gms. Lactose mgs.)l500 gms. Acacia (3 mgs.)-30 gms. Starch, bolted (65 mgs.)650 gms. Calcium stearate (3 mgs.)30 gms.

The first three ingredients are powdered and mixed well. The mixture is granulated with syrup-starch paste and dried. The dried granules are well mixed with a starch-calcium stearate lubricant mixture. The whole is compressed into tablets.

Good results are obtained in the prevention of the estrual period in smaller dogs weighing about 5 lbs., one table being administered daily.

EXAMPLE 8 Tablet 10,000 tablets for oral administration are prepared from the following types and amounts of ingredients. Each tablet contains 25 mgs. of the active ingredient.

6-chloro-17ot-hydroxy-4,6-pregnadiene 3,20 dione 17- acetate250 gms. Lactose2450 gms.

The finely powdered steroid and lactose are mixed well and granulated with syrup-starch paste. Starch and calcium stearate are used as lubricants in the compressing step.

The tablets are administered orally 3 times daily with good results in the treatment of habitual and threatened abortion in humans.

Similarly, tablets, each containing 10 mgs. of the steroid, are prepared for the administration of smaller dosages.

10,000 mls. of a sterile aqueous suspension are prepared from the following types and amounts of in gredients:

Each ml.:

6-chloro-17u-hydroxy-4,6-pregnadiene 3,20 dione l7-acetate (10 mgs.)100 gms.

Sodium chloride (9 mgs.)90 gms.

Preservative (0.2 mg.)2 gms.

Water for injection U.S.P. (q.s.), ad.1-0,000 mls.

The sodium chloride and preservative are dissolved in the water and the whole is sterilized by passage through a sterilizing filter. The steroid is micronized, sterilized by exposure to sterilizing vapor and added aseptically to the sterile aqueous solution. Dispersion is accomplished by mixing through a sterile homogenizer. The final suspension is filled aseptically into sterile vials. The duration of action of the suspension is prolonged. Beneficial results in the treatment of endometriosis and recurrent abortion in humans are obtained by the injection of 1 ml. one to three times monthly. Inhibition of ovulation can be brought about by like dosages.

EXAMPLE 10 Oral Suspension An aqueous suspension for oral administration, containing in each teaspoonful (approximately mls.) 2.5 mgs. of -chloro-l7ot-hydroxy-4,6-pregnadiene-3,20-dione 17-acetate, is prepared from the following types and amounts of ingredients:

6-chloro-17u-hydroxy-4,fi-pregnadiene 3,20 dione 17- acetate0.5 gm.

Preservative-2 gms.

Flavorq.s.

Purified water U.S.P., q.s. ad.1000 mls.

The preservative and flavor are dissolved in the water. The finely powdered steroid is added and the Whole is homogenized.

A daily dose of 1 teaspoonful (5 mls.) gives good results in the treatment of menstrual disorders in humans.

EXAMPLE 11 Hard gelatin capsule 1000 hard gelatin, two-piece capsules for oral administration, each containing 300 mgs. of 6-chloro-17ochydroxy-4,6-pregnadiene-3,20-dione 17 -acetate, are prepared from the following types and amounts of materials:

6-chloro-17a-hydroxy-4,6-pregnadiene 3,20 dione 17- acetate-300 gms.

The micronized steroid is encapsulated by the usual techniques in two-piece capsules.

A daily dose of 1 capsule gives good results in the control of the estrual period in a mare. After cessation of treatment, the mares can be bred successfully at approximately the same time.

EXAMPLE 12 Ready-mix feed composition Ready-mixed feed is prepared in the following manner:

Commercial dog feed-100 lbs. 6-chloro-17a-hydroxy-4,6-pregnadiene-3,20-dione 17-acetate600 mgs.

The steroid is worked into a portion of the feed by careful mixing and milling. This mix is incorporated uniformly into the remaining feed. Each pound of the finished preparation contains 6 mgs. of the steroid providing a total daily dose of 7.5 mgs. for a kilo dog eating 1% lbs. of the feed per day. This daily dose is effective in preventing estrus in the female dog.

8 EXAMPLE 13 Ingestible pre-mix Following the procedure of Example 5, a pre-mix is prepared to provide 0.5 mg. of 6-chloro-17 -hydroxy-4,6 pregnadiene-lZO-dione 17-acetate per pound of ration;

Individual feeding of dairy heifers of known reproductive history was studied. Feeding began on the 15th day of the estrual cycle and continued through day 30.:Twice daily observations for estrus and rectal palpation of the ovaries provided data on the elfectiveness of thetreatment.

Once daily feedings equivalent to 4'mgs. of the essential active ingredient inhibited ovulation. With feedings equivalent to 4 mgs. per day, the average number of days for return to estrus. was 7.8 days after cessation of treatment.

EXAMPLE 14 lnjectable suspension 10,000 mls. of a sterile aqueous suspension are prepared from the following types and amounts of ingredients:

Each ml. 1

fiu-chloro-l7m-hydroxy-4-pregnene-3,20-dione 17-acetate (250 mgs.)--2500 gms. Sodium chloride (mgs.)-- gms. Water for injection U.S.P. (q.s.) ad.l0,000 mls.

The sodium chloride and a preservative are dissolved in the water and the whole is sterilized by passage through a sterilizing filter. The active ingredient is micronized, sterilized by exposure to sterilizing vapor and added aseptically to the sterile aqueous solution. Dispersion is accomplished by passing through a sterile homogenizer. The final suspension is filled aseptically into sterile vials.

The duration of action of the injected suspension is prolonged. The single injection of 4 mls. per animal in a group of beef cattle is eifective in preventing estrus for from about 50 to about days.

EXAMPLE 15 Oral suspension An aqueous suspension for oral administration, containing in each teaspoonful (approximately 5 mls.) 25 mgs. of 6a.-chloro-17m-hydroxy-4-pregnene-3,20-dione 17- acetate, is prepared from the following types and amounts of ingredients:

60c chloro 17a-hydroxy-4-pregnene-3,20-dione 17-acetate5 gms.

Preservative2 gms.

Flavorq.s.

Purified water U.S.P., q.s. ad.l000 mls.

The finely powdered steroid is added and the Whole is homogenized.

A daily dose of 1 teaspoonfnl v(5 mls.) gives good results in the treatment of menstrual disorders in humans.

Natural and synthetic estrogens, i.e., substances capable of inducing feminine characteristics, are useful supplementary active ingredients in the above examples for oral use, especially to maintain a normal balance between progestational and estrogenic activity and in the prevention of ovulation in humans. Such estrogens include estradiol, ethinyl estradiol, benzestrol, dienestrol, diethylstilbestrol, hexestrol, and the like. Per dose, the respective amounts thereof are 0.1 to 0.5 mg., 0.01 to 0.5 mg., 0.5 to 25 mgs., 0.1 to 10 mgs., 0.1 to 25 mgs., and 1 to 3 mgs.

What is claimed is:

1. A method of synchronizing estrual periods in a group of ovulating animals which comprises systemic administration thereto of an effective dose of 6-chlorol7u-hydroxy-4,6-pregnadiene-3,20-dione l7-acetate in a dosage unit form.

2. A method of controlling the moulting period and egg-laying period in laying hens which comprises oral 9 hydroxy-4,6-pregnadiene-3,ZO-dione l7-acetate in a dosage unit form.

3. A method of prolonged prevention of estrualperiods in ovulating animals which comprises the oral administra tion thereto of an effective dose of 6-chloro-17a-hydroxy- 4,6-pregnadiene-3,20-dione l7-a'cetate in a dosage unit form.

4. A method of prolonged prevention of estrual periods in ovulating animals which comprises the parenteral administration thereto of an effective dose of 6-Chl01'0-17cchydroxy-4,6-pregnadiene-3,20-dione 17-acetate in a dosage unit form.

5. A method for the hormonal control of the reproductive cycle in an ovulating mammal which comprises sys temic administration thereto of an effective dose of 6- chloro 17a-hydroxy-4,6-pregnadiene-3,20-dione 17-acetate in a dosage unit form.

6. The method of claim which includes as an additional active ingredient from about 0.01 mg. to about 25 mg. of a member selected from the group consisting of natural and synthetic estrogens.

7. A method of hormonal control of the reproductive cycle in an ovulating bird which comprises systemic administration thereto of an efiective dose of 6-chloro-17ahydroxy-4,6-pregnadiene-3,20-dione 17-acetate in a dosage unit form.

8. The method of claim 7 which includes as an additional active ingredient from about 0.01 mg. to about 25 References Cited UNITED STATES PATENTS 3,452,058 6/1969 Ringold et al 260397.4 2,838,531 6/1958 Babcock et a1 424243 2,838,549 6/1958 Herr ct al 424243 2,895,875 7/ 1959 Klette 424243 3,040,065 6/ 1962 Schneider et a1 424243 3,068,246 12/ 1962 Magerlein et al 424243 3,131,200 4/ 1964 Reirnann et al 424243 OTHER REFERENCES Ring0ldJ.A.C.S., vol. 81, 1959, pp. 3485 and 3486. Veterinary Bulletin, vol. 23, 1957.

'Greenblatt: Ofiice Endocrinology, fourth edition, p. 552.

RICHARD L. HUFF, Primary Examiner 

